Inogen

Quality Engineer III

Job Description

Posted on: 
2025-08-18

Responsibilities

  • Drive new product design and development activities.
  • Lead the effective transition from product design to production.
  • Oversee manufacturing and quality activities for improvement and risk.
  • Achieve quality initiatives and manage post-market activities.
  • Conduct root cause investigations and implement corrective actions.
  • Develop and implement quality management system procedures.
  • Participate in internal and external audits and supplier qualification activities.

Job Requirements

  • Bachelor's degree in engineering or related scientific field.
  • Minimum of three years of experience as a Quality Engineer in the medical device industry.
  • Strong understanding of FDA QSR and EU MDR regulations.
  • Proficiency in statistical analysis software like Minitab.
  • Excellent communication and organizational skills.
  • Ability to work onsite and collaborate across departments.
  • Experience in risk management and process validation activities.
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